Tamara Žigman

2PUBLICATIONS
1CO-AUTHORS
Neonatology
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (2)

|Nov 12, 2020
ATP synthase deficiency due to m.8528T>C mutation - a novel cause of severe neonatal hyperammonemia requiring hemodialysis.

Tamara Žigman, Katarina Šikić, Danijela Petković Ramadža

|Sep 23, 2018
Hypogammaglobulinemia and imaging features in a patient with infantile free sialic acid storage disease (ISSD) and a novel mutation in the SLC17A5 gene.

Tamara Žigman, Danijela Petković Ramadža, Mario Lušić

Pageof 1

Frequent Collaborators

1 joint publications

Dorotea Ninković